Label: DAILY FACIAL MOISTURIZER SPF 25- sunscreen cream

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 2, 2018

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  • Uses

    -Moisturizes and helps to relieve irritated and sensitive skin

    -Higher SPF gives more sunburn protection

    -Water resistant

  • Keep Out of the Reach of Children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Warnings

    For external use only

  • .Stop Use

    Stop Use and ask a Doctor if a rash rash or irritation develops and lasts

  • Questions

    Questions? Please call 1 (800) 423-2341

  • Inactive Ingredients

    Purified Water, Propylene Glycol Dioctanoate, Petrolatum, Glycerin, Glyceryl Stearate, PEG-100 Stearate, DEA-Cetyl Phosphate, Stearic Acid, Hyaluronic Acid, Benzyl Alcohol, Dimethicone, Cyclomethicone, PVP/Eicosene Copolymer, Silica, Sodium Carbomer 941, Allantoin, Disodium EDTA, Magnesium Aluminum Silicate

  • Other Information

    -High sun protection product

    -Sun Alert: limiting sun exposure, wearing sun protective clothing and using sunscreens may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

    -Avoid exposure to extreme heat or cold.

  • Active Ingredients

    Octinoxate......7.5% Sunscreen

    Homosalate....6.0% Sunscreen

    Avobenzone...3.0% Sunscreen

    Octocrylene....1.5% Sunscreen

  • Directions

    -Apply DML Daily Facial Moisturizer liberally and evenly 15-20 minutes before sun exposure and message in gently, allowing it to dry. Reapply as needed or as directed by your Dermatologist.

    -DML Daily Facial is an excellant make-up base.

  • Purpose

    Sunscreen

  • Package Label Principal Display Panel

    DML Facial Moisturier

  • INGREDIENTS AND APPEARANCE
    DAILY FACIAL MOISTURIZER  SPF 25
    sunscreen cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0096-0721
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE0.06 g  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE0.03 g  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.075 g  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE0.015 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE 1000 (UNII: MCU2324216)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0096-0721-077 g in 1 BOTTLE; Type 0: Not a Combination Product08/01/1991
    2NDC:0096-0721-4545 g in 1 BOTTLE; Type 0: Not a Combination Product08/01/1991
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35208/01/1991
    Labeler - Person and Covey (008482473)
    Establishment
    NameAddressID/FEIBusiness Operations
    Person and Covey008482473manufacture(0096-0721)
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